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NCT07109557
The Effect of Baduanjin on Patients Undergoing Knee Replacement Surgery
NA trial testing Baduanjin in Pain, Postoperative in 60 participants. Currently enrolling.
1 July 2026
Quick facts
| Lead sponsor | Niran Çoban |
|---|---|
| Phase | NA |
| Status | Recruiting now |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | single |
| Primary purpose | supportive care |
| Enrollment | 60 |
| Start date | 1 July 2025 |
| Primary completion | 1 July 2026 |
| Estimated completion | 1 December 2026 |
| Sites | 1 location across Turkey (Türkiye) |
Drugs / interventions tested
- Baduanjin
Conditions studied
- Pain, Postoperative — all drugs for Pain, Postoperative →
- Surgery — all drugs for Surgery →
- Knee Replacement — all drugs for Knee Replacement →
- Nurse's Role — all drugs for Nurse's Role →
Sponsor
Niran Çoban
Who can join
Adults 18 to 70, any sex, with Pain, Postoperative or Surgery. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
This randomized controlled trial aims to evaluate the effects of Baduanjin, a traditional Chinese mind-body exercise, on pain, comfort, and quality of recovery in patients undergoing total knee arthroplasty (TKA). The study will be conducted between July 2025 and July 2026 at Yalova Training and Research Hospital's Orthopedics Clinic. Sixty patients will be randomly assigned into two groups: an intervention group practicing Baduanjin and a control group receiving standard postoperative care. The intervention will begin on the first postoperative day and continue for three weeks. Outcome measures include the Visual Analog Scale (VAS) for pain, the General Comfort Questionnaire, and the Quality of Recovery-40 (QoR-40) questionnaire. These assessments will be conducted weekly for three weeks. The control group will follow routine postoperative care without Baduanjin. The primary objective is to determine whether Baduanjin can improve postoperative outcomes in terms of pain reduction, increased comfort, and better recovery quality.
Publications & conference data
No peer-reviewed publications indexed yet for this trial.
Verify or expand the search:
- PubMed search for NCT07109557
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
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Related trials
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Trials testing the same drug.
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- NCT07015658 — Clinical Effects of Moxibustion Combined With Tailored Baduanjin Exercise Programs on Early Postoperative Rehabilitation · NA · not yet recruiting
- NCT06803459 — Effects of Baduanjin and PNF on Upper Crossed Syndrome Among University Students in Henan Province,China · NA · completed
Other recruiting trials for Pain, Postoperative
Currently open trials in the same condition.
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- NCT06740214 — Analgesic Efficacy of Different Liposomal Bupivacaine Doses in the Adductor Canal Block for Total Knee Arthroplasty · Phase 3 · recruiting
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Other Niran Çoban trials
Trials by the same sponsor.
- NCT07109492 — The Role of Mandala Painting Before Surgery · NA · recruiting
- NCT07171008 — The Effect of Ney Music on Patients Undergoing Lumbar Disc Surgery · NA · recruiting
- NCT05711706 — Su Jok Application in After Lumbar Disc Surgery · NA · completed
Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT07109557 (US National Library of Medicine, public domain)
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Niran Çoban
- Last refreshed: 12 August 2025
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT07109557.
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